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2007
Se, H. C., Leight, S. N., Lee, V. M. - Y., Li, T., et al. (2007). Accelerated Aβ deposition in APPswe/PS1ΔE9 mice with hemizygous deletions of TTR (transthyretin). Journal of Neuroscience, 27(26), 7006 - 7010.
Wong, J., Obst, R., Correia-Neves, M., Losyev, G., et al. (2007). Adaptation of TCR repertoires to self-peptides in regulatory and nonregulatory CB4 + T cells. Journal of Immunology, 178(11), 7032 - 7041.
Martins, S., Calafell, F., Gaspar, C., Wong, V. C. N., et al. (2007). Asian origin for the worldwide-spread mutational event in Machado-Joseph disease. Archives of Neurology, 64(10), 1502 - 1508.
Martins, S., Calafell, F., Gaspar, C., Wong, V. C. N., et al. (2007). Asian origin for the worldwide-spread mutational event in Machado-Joseph disease. Archives of Neurology, 64(10), 1502 - 1508.
Gobec, S., Plantan, I., Mravljak, J., Švajger, U., et al. (2007). Design, synthesis, biochemical evaluation and antimycobacterial action of phosphonate inhibitors of antigen 85C, a crucial enzyme involved in biosynthesis of the mycobacterial cell wall. European Journal of Medicinal Chemistry, 42(1), 54 - 63.
Benninger, Y., Thurnherr, T., Pereira, J. A., Krause, S., et al. (2007). Essential and distinct roles for cdc42 and rac1 in the regulation of Schwann cell biology during peripheral nervous system development. Journal of Cell Biology, 177(6), 1051 - 1061.
Altland, K., Benson, M. D., Costello, C. E., Ferlini, A., et al. (2007). Genetic microheterogeneity of human transthyretin detected by IEF. Electrophoresis, 28(12), 2053 - 2064.
Normand, P., Lapierre, P., Tisa, L. S., Gogarten, J. P., et al. (2007). Genome characteristics of facultatively symbiotic Frankia sp. strains reflect host range and host plant biogeography. Genome Research, 17(1), 7 - 15.
Normand, P., Lapierre, P., Tisa, L. S., Gogarten, J. P., et al. (2007). Genome characteristics of facultatively symbiotic Frankia sp. strains reflect host range and host plant biogeography. Genome Research, 17(1), 7 - 15.
Weber, E. M., Olsson, A. S., & Algers, B. (2007). High mortality rates among newborn laboratory mice - Is it natural and which are the causes?. Acta Veterinaria Scandinavica, 49(SUPPL. 1).
Gardenghi, S., Marongiu, M. F., Ramos, P., Guy, E., et al. (2007). Ineffective erythropoiesis in β-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin. Blood, 109(11), 5027 - 5035.
Endt, J., Mccann, F. E., Almeida, C. R., Urlaub, D., et al. (2007). Inhibitory receptor signals suppress ligation-induced recruitment of NKG2D to GM1-rich membrane domains at the human NK cell immune synapse. Journal of Immunology, 178(9), 5606 - 5611.
Williams, G. S., Collinson, L. M., Brzostek, J., Eissmann, P., et al. (2007). Membranous ctructures transfer cell surface proteins across NK cell immune synapses. Traffic, 8(9), 1190 - 1204.
Williams, B., Leung, G., Maiato, H., Wong, A., et al. (2007). Mitch - A rapidly evolving component of the Ndc80 kinetochore complex required for correct chromosome segregation in Drosophila. Journal of Cell Science, 120(20), 3522 - 3533.
Williams, B., Leung, G., Maiato, H., Wong, A., et al. (2007). Mitch - A rapidly evolving component of the Ndc80 kinetochore complex required for correct chromosome segregation in Drosophila. Journal of Cell Science, 120(20), 3522 - 3533.
Williams, B., Leung, G., Maiato, H., Wong, A., et al. (2007). Mitch - A rapidly evolving component of the Ndc80 kinetochore complex required for correct chromosome segregation in Drosophila. Journal of Cell Science, 120(20), 3522 - 3533.
Olsson, I. A. S., & Westlund, K. (2007). More than numbers matter: The effect of social factors on behaviour and welfare of laboratory rodents and non-human primates. Applied Animal Behaviour Science, 103(3-4), 229 - 254.
Karageorgos, L., Brooks, D. A., Pollard, A., Melville, E. L., et al. (2007). Mutational analysis of 105 mucopolysaccharidosis type VI patients. Human Mutation, 28(9), 897 - 903.
Stevanin, G., Paternotte, C., Coutinho, P., Klebe, S., et al. (2007). A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21. Neurology, 68(21), 1837 - 1840.
Couto, A. R., Bruges-Armas, J., Peach, C. A., Chapman, K., et al. (2007). A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis. Calcified Tissue International, 81(2), 81 - 84.
Stendel, C., Roos, A., Deconinck, T., Pereira, J., et al. (2007). Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4. American Journal of Human Genetics, 81(1), 158 - 164.

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